Gardner DK, Rodriegez - Martinez H, Lane M. Fetal development after transfer is increased by replacing protein with the glycosaminoglycan hyaluronan for
mouse embryo culture and transfer.
Not exact matches
The team set up a microscope and video camera over several
culture dishes, each containing a single neural progenitor cell taken from a
mouse embryo 10 days after fertilization.
Sensory and sympathetic ganglia were dissected out of eight - day - old chick
embryos and
cultured in a semisolid medium in proximity to fragments of
mouse sarcoma - 180 tumors.
For Noggin protein - treated caps, stage 9 animal cap explants were
cultured with 500 nM
mouse Noggin protein (Sigma - Aldrich, catalogue number N6784) in 0.7 × MMR and 50 µg / ml gentamicin sulphate and grown to sibling
embryo stage 15 for transplantation.
They then inserted the spatially oriented human stem cells (human rsPSCs) into specific regions of partially dissected
mouse embryos and
cultured them in a dish for 36 hours.
We exploit chick and
mouse embryo animal models, combined with live imaging, cell and tissue
cultures and molecular approaches.
We prefer to
culture our cells on
mouse embryo fibroblasts (MEFs) but occasionally grow the cells feeder free for particular applications, such as nucleofection, viral transduction or karyotyping.
Ex vivo cortical electroporation (E15
mouse embryos) coupled with organotypic
culture for 5 days results in radial migration of EGFP + pyramidal neurons to the cortical plate (CP) and the projection of their axon in the intermediate zone (IZ).
Scientists at the University of Cambridge have managed to create a structure resembling a
mouse embryo in
culture, using two types of stem cells — the body's «master cells» — and a 3D scaffold on which they can grow.
For instance, MEF cells are usually made of fibroblasts from the
mouse embryos at embryonic day 13.5 and only cells at early passages (p2 to p3) are used as feeders for derivation and
culture of embryonic stem (ES) and iPS cells.
Differential effects of
culture on imprinted H19 expression in the preimplantation
mouse embryo
The GEM Facility will thaw one straw of frozen
embryos and
culture overnight to the blastocyst stage to insure that
embryo freezing is feasible for that particular
mouse line.
Effect of stem cell activation,
culture media of manipulated
embryos, and site of
embryo transfer in the production of F0 embryonic stem cell
mice
Culture of preimplantation
mouse embryos affects fetal development and the expression of imprinted genes
It has also been reported that
culture and transfer of
mouse preimplantation
embryos resulted in altered postnatal growth and organ sizing in the offspring that persisted into a second generation, suggesting heritable epigenetic modifications [11].
Thus, although the cells of the inner cell mass of the
mouse embryo all express the pluripotency factor Oct - 4, neither the inner cell mass nor
cultures of
mouse ES cells show uniform expression of the pluripotency factor nanog [6], [7].
One - cell
embryos obtained from superovulated female
mice mated with (C57BL / 6xCBA) males were
cultured in KSOM media (Sigma - Aldrich) supplemented with 10 % FCS (Sigma - Aldrich) for 4 days.